Canonical Allele Identifier: PA645429065
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 221623
ClinVar RCV Id: RCV000416904 RCV000649006 RCV003488462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Arg200Cys
CA3771446
NM_021922.3:c.598C>T